We have examined the polymer/surfactant interaction in mixed aqueous solutions of cationic surfactants and anionic polyelectrolytes combining various techniques: tensiometry, potentiometry with surfactant-selective electrodes, and viscosimetry. We have investigated the role of varying polymer charge density, polymer concentration, surfactant chain length, polymer backbone rigidity, and molecular weight on the critical aggregation concentration (Cac) of mixed polymer/surfactant systems. The Cac of these systems, estimated from tensiometry and potentiometry, is found to be in close agreement. Different Cac variations with polymer charge density and surfactant chain length were observed with polymers having persistence lengths either smaller or larger than surfactant micelle size, which might reflect a different type of molecular organization in the polymer/surfactant complexes. The surfactant concentration at which the viscosity starts to decrease sharply is different from the Cac and probably reflects the polymer chain shrinkage due to surfactant binding.

Highly water-repellent surfaces have been prepared from arrayed nanowires of zinc oxide (ZnO) by a treatment with stearic acid. The layers are electrochemically deposited on a nanocrystalline seed layer from an oxygenated aqueous zinc chloride solution. An advancing contact angle (CA) as high as 176° is obtained with a very small hysteresis ∼1°. These results, supplemented by infrared spectroscopy, show that the stearic acid forms a very well-packed self-assembled monolayer. The CA measurements show a very good stability of the treated surface even when exposed to harsh conditions or long-term ambient illumination.